Diagnostic test strip for collecting and detecting an analyte in a fluid sample

ABSTRACT

A test strip for the use of the determination of an analyte in a fluid sample according to one embodiment of the present invention is disclosed. The test strip comprises of a base having a top and a bottom, a collection chamber that extends between the top and the bottom of the base, a containing ring that is disposed on the bottom of the base and surrounds the collection chamber, and a capillary channel formed in top of the base that has an inlet fluidly coupled to the collection chamber and a test element disposed within the capillary channel. A lid is attached to the top of the base and covers the collection chamber, the test area, and at least a portion of the capillary channel.

This application claims benefit of U.S. Provisional Application Ser. No.60/473,720 filed on May 29, 2003.

FIELD OF THE INVENTION

The present invention relates generally to diagnostic instruments and,more particularly, to a diagnostic test strip for use in determining theconcentration of an analyte in a liquid sample.

BACKGROUND OF THE INVENTION

Test strips (e.g., biosensors) containing reagents are often used inassays for determining the concentration of an analyte in a fluidsample. Testing and self-testing for the concentration of glucose inblood is a common use for test strips. One method of obtaining a bloodsample and analyzing the sample for determining the glucose level iswith a lancing device and a separate blood collection device. Inobtaining a blood sample, a drop of blood is obtained from the fingertipusing the lancing device, and the blood is harvested using a test strip,which is then analyzed by a test unit that determines the concentrationof glucose in the blood. Test strips are also used for determining theconcentration or presence of various other analytes (e.g., fructosamine,hemoglobin, cholesterol, glucose, alcohol, drugs including illegaldrugs, etc.) in a variety of body fluids (e.g., blood, interstitialfluid, saliva, urine, etc.).

A drawback associated with the use of physically separate lancing andcollection devices is that a patient/user must manipulate two differentinstruments requiring the user/patient to bring the collection device(e.g., the test strip) to the area of skin that has been lanced tocollect the sample. Because the user must align the collection devicewith the sample to be collected, a larger than necessary amount ofsample often is produced and collected to ensure an accurate analysis.In other situations, not enough sample is collected for accurateanalysis because the collection device is not properly positioned. Thisproblem can be further compounded if the user has impaired vision orpoor dexterity. Because test systems are requiring smaller volumes ofblood for analysis, it is difficult to position a collection instrumentfor proper collection.

The surface condition of the skin affects the formation of a blooddroplet at the lancet site on skin. Many individuals use hand lotions,have oily or sweaty skin, or do not dry their hands completely afterwashing which also affects droplet formation. Often users do not alwayscleanse the area of skin to be lanced with alcohol. These variationsincrease the wettability of the skin's surface causing the droplet tospread in an uncontrolled and unpredictable manner making it difficultto harvest the sample.

Further, the collection of blood samples on alternative sites such asthe forearm is complicated by the presence of body hair because thesample (e.g., blood) has a tendency to “wick up” the hairs found onthese parts of the body. Cleaning the lance site with alcohol does notalleviate this wicking problem. Thus, there exists a need for a lancingand collection device that co-locates the lancet and the collectionpoint to accurately collect a blood sample for analysis.

SUMMARY OF THE INVENTION

A test strip for the use of the determination of an analyte in a fluidsample according to one embodiment of the present invention isdisclosed. The test strip comprises a base having a top and a bottom, acollection chamber that extends between the top and the bottom of thebase, a containing ring that is disposed on the bottom of the base andsurrounds the collection chamber, and a capillary channel formed in topof the base that has an inlet fluidly coupled to the collection chamber,and test element disposed within the capillary channel. A lid isattached to the top of the base and covers the collection chamber, thetest membrane, and at least a portion of the capillary channel.

The above summary of the present invention is not intended to representeach embodiment, or every aspect, of the present invention. Additionalfeatures and benefits of the present invention will become apparent fromthe detailed description, figures, and claims set forth below.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an upper perspective view of a portion of a test stripaccording to one embodiment of the present invention.

FIG. 2 is a lower perspective view of the test strip of FIG. 1.

FIG. 3 is a perspective view of a test strip integrated into a lancingand harvesting device according to one embodiment of the presentinvention.

FIG. 4 is a side view of a lancing and harvesting device and end capaccording to another embodiment of the present invention.

FIG. 5 a-5 f are oversized perspective and side views of a forward endof a lancing and harvesting device illustrating various points duringthe lacing of a test subject's skin and the subsequent sample harvestingaccording to one embodiment of the present invention.

FIG. 6 is a top perspective view of a test strip according to oneembodiment of the present invention.

While the invention is susceptible to various modifications andalternative forms, specific embodiments are shown by way of example inthe drawings and are described in detail herein. It should beunderstood, however, that the invention is not intended to be limited tothe particular forms disclosed. Rather, the invention is to cover allmodifications, equivalents and alternatives falling within the spiritand scope of the invention as defined by the appended claims.

DESCRIPTION OF ILLUSTRATED EMBODIMENTS

Turning now to the drawings and initially to FIGS. 1 and 2, a test strip10 is shown according to one embodiment of the present invention. Thetest strip 10 includes a base 12 and a lid 14. The base 12 has a lowersurface 13 and an upper surface 15. The base 12 includes a collectionchamber 16, a capillary channel 18 that includes a test area 19, and acontaining ring 24. The capillary channel 18 is extended beyond the testarea 19 to form an optional vent 22. The lid 14 covers the collectionchamber 16 and the capillary channel 18 including the test area 19. Thelid 14 is adhered to the base 12 according to one embodiment of thepresent invention. A test element 20, which includes a regent for use inan assay, is disposed in the test area of the capillary channel 18. Thetest strip 10 may be incorporated into a lancing and harvesting device26 (FIG. 4) according to one embodiment of the present invention as willbe described in detail in connection with FIGS. 4-5 f.

The collection chamber 16 and the capillary channel 18, which includesthe test area and the vent 22 (if any), may be embossed upon the uppersurface 15 of the base 12, but may also be formed in the molding of thebase 12, by machining, or through another suitable manufacturing method.In the illustrated embodiment, the collection chamber 16 is acylindrical aperture extending through the base 12. The inlet of thecapillary channel 18 is formed in the side wall of the collectionchamber 16. The capillary channel 18 fluidly couples the collectionchamber 16 and the test area 19 containing the test element 20. Thecollection chamber 16, the capillary channel 18 including the test area19, or a combination thereof may be coated with a hydrophilic materialto promote movement of the fluid sample. Additionally, according to oneembodiment of the present invention, the capillary channel 18 isappropriately sized to provide under-fill protection.

In one embodiment of the present invention, a test element 20 isattached to the lid 14 with an adhesive, which is substantially clear inembodiments wherein the test element 20 is optically read through thelid 14. In embodiments where the test element 20 is adhered to the lid14, the test area 19 of the capillary channel 18 is dimensioned toprovide a slight clearance between the bottom of the test area 19 andthe bottom of the test element 20 so that the fluid sample is exposed tomore surface area of the test element 20. Similarly, the test area 19 ofthe capillary channel 18 may be dimensioned to provide for clearancearound the edge of the test element 20 as is shown in FIG. 1, forexample. In alternative embodiments of the present invention, the testelement can be attached to the base 12.

In the collection of a body fluid sample, such as blood, from a testsubject, the lower surface 13 of the base 12 is placed on the testsubject's skin. A containing ring 24, which surrounds the collectionchamber 16 and downwardly extends from the lower surface 13 of the base12, contacts the test subject's skin. As will be described in detailbelow, the test subject's skin is punctured within the periphery of thecollection chamber 16. The containing ring 24 inhibits the spreading ofthe sample across the skin and maintains the sample within the peripheryof the collection chamber 16. The containing ring 24 is formed duringthe molding of the base 12, is embossed upon the lower surface 13, or isotherwise attached to the lower surface 13 of the base 12 duringmanufacturing.

The base 12 can be composed of any suitable material such as, forexample, polycarbonate, polypropylene, polystyrene, etc. The lid 14 isconstructed of any suitable material as required by the nature of theanalysis to be performed. For example, if an optical analysis isdesired, the lid 14 may be constructed of a substantially opticallyclear material such as polyethylene terephthalate (PET) orpolycarbonate, for example. Alternatively, for applications where theopacity of the lid 14 is not relevant, the lid 14 may be constructed ofpolycarbonate, polypropylene, polystyrene, and polyethyleneterephthalate (PET). The lid material is substantially nonporous so thatthe lid does not absorb the sample; rather, the lid directs the sampleto the inlet of the capillary channel 18 as described below.

The test strip 10 may be implemented into a variety of lancing devicesaccording to alternative embodiments of the present invention. Examplesof lancing devices that may be used with various embodiments of thepresent invention include those described in U.S. Pat. No. 5,152,942(“Vacuum Assisted Lancing Device”); U.S. Pat. No. 5,350,392 (“LancingDevice with Automatic Cocking”); and U.S. Pat. No. 6,364,889(“Electronic Lancing Device”); each of which is incorporated herein byreference in its entirety. The implementation of a test strip 10 with alancing device 26 enable the lancing device 26 to lance the skin of atest subject and to harvest the body fluid sample from the lancet site.

Referring now to FIG. 3, the forward end of a lancing and harvestingdevice 26 that implements a test strip 10 is shown according to oneembodiment of the present invention. The test strip 10 can take on avariety of shapes and configurations to conform with numerous instrumentconcepts, while operating as described above. For example, while FIG. 3shows the test strip 10 being dimensioned substantially the same as thecross-section of the end cap 30, the test strip 10 can be generallyrectangular-shaped as shown in FIGS. 1-2. The test strip 10 may beattached to an end cap 30, which is removably attached to the lancingdevice 26. The lancing and harvesting device 26 contains a lancet 28 forpuncturing both the lid 14 and the skin of the subject as is describedbelow.

Referring now to FIG. 4, the lancing and harvesting device 26 thatimplements a test strip 10 is shown according to one embodiment of thepresent invention. The lancing assembly includes a body 32 that houses alancing assembly 31 having a plunger 34 for driving the lancet 28 and atop end 36 that the plunger 34 extends beyond the housing 32. In usingthe lancet 28 to puncture a test subject's skin, a user grasps thedevice 26 by the body 32 and depresses the top end 36 of the plunger34—moving the plunger 34 into the body 32 of the device 26—to downwardlyadvance the lancet 28 into a test subject's skin. A lancet holder (notshown) is disposed within the body 32. The lancet 28 is removablyattached to the lancet holder so that the lancet 28 may be detached anddiscarded after use. Within the housing 32, an opposite end of thelancet holder is coupled to the plunger 34. Thus, the plunger 34 movesthe lancet holder which, in turn, drives the lancet 28.

The end cap 30 attaches to a forward end 40 of the device 26 oppositethe plunger 34. A rim 42 of the end cap 30 removably attaches to theforward end 40 of the plunger 34. (The forward end 40 includes an O-ringaccording to vacuum-assisted embodiments of the lancing device 26 forforming an airtight seal between the end cap 30 and the forward end 40.)An open end 44 of the end cap 30 includes an aperture 46 through whichthe lancet 28 passes to puncture a test subject's skin. In oneembodiment of the invention, the end cap 30 contains an aperture 45 inits sidewall for inserting and removing a test strip 10. In anotherembodiment of the present invention, the test strip 10 is fixedlyattached to the end cap 30, which is disposable such that removing theend cap 30 also removes the used test strip 10.

During the lancing of a test subject's skin, the open end 44 of the endcap 30 is placed on an area of the test subject's skin (e.g., a forearm,a finger, etc.). The plunger 34 is depressed to advance the lancet 28from a retracted position wherein the lancet 28 is completely containedwithin the end cap 30, to a lancing position wherein the lancet 28extends through the aperture 46 in the end cap 30. Movement of theplunger 34 by the user triggers a spring (not shown) within the body 32of the lancing assembly 31 that rapidly advances the lancet 28 into atest subject's skin. The lancing assembly 31 includes a second spring(not shown) for moving the lancet 28 back toward the retracted position.

In the embodiment shown in FIG. 4, the lancing assembly 31 furtherincludes an instrument 48 for reading the test strip 10 (not shown) anddetermining the analyte concentration in the sample. The instrument 48includes a display 50 for communicating the results of the assay to theuser. In embodiments of the present invention that do not include theinstrument, a separate device is used for reading the test strip 10.

According to one embodiment of the present invention, the lancing device26 is vacuum assisted as described in U.S. Pat. No. 5,152,942(incorporated by reference above) to facilitate the production of ablood sample at the puncture site on the test subject's skin. In such anembodiment, the rim 42 of the end cap 30 forms an airtight seal with theuse of an O-ring as is described above. And an airtight seal is createdbetween the open end 44 of the end cap 30 and the test subject's skin bypressing the end cap against the skin. The lancing assembly 31 includesa vacuum member (not shown) such as a diaphragm or bellows thatdisplaces air within the lancing assembly and end cap 30 to form avacuum within the end cap 30. During the lancing operation, release ofthe plunger 36 by the user triggers the vacuum member which evacuatesair from the end cap 30.

As discussed above, the test element 20 contains a reagent for use indetermining the concentration of the analyte of interest in a sample.The reagent is designed to react with the analyte in the sample. Thatreaction is indicative of the analyte concentration in the sample andcan be measured by an appropriate sensor. The specific reagentincorporated into the test element 20 is a function of the analyte, andthe type of assay to be used for determining the concentration of theanalyte.

According to one embodiment of the present invention, the reagentapplied to the test element 20 is designed to produce a colorimetricreaction indicative of the analyte concentration as is known in the art.An optical readhead or detector is used to measure the degree of thecolor change for determining the concentration of the analyte. Accordingto one embodiment of the present invention, a light detector is disposedwithin the end cap 30 of the device 26 for reading the test strip.Colorimetric testing is described in detail in U.S. Pat. No. 6,181,417B1 (entitled “Photometric Readhead with Light Shaping Plate”); U.S. Pat.No. 5,518,689 (entitled “Diffuse Light Reflectance Readhead”); and U.S.Pat. No. 5,611,999 (entitled “Diffuse Light Reflectance Readhead”); eachof which is incorporated herein by reference in its entirety.

Alternatively, the reagent applied to the test element 20 is designed toproduced an electrochemical reaction indicative of the analyteconcentration in the sample as is known in the art. In anelectrochemical assay, the regent is designed to react with the analyteto create an oxidation current at electrodes disposed within the testarea 19 which is directly proportional to the concentration of glucosein the user's blood. The resulting current can be measured by a meter,such as a meter incorporated in to the instrument 48. Electrochemicaltesting is described in U.S. Pat. No. 5,120,420 (entitled “Biosensor anda Process for Preparation Thereof”); U.S. Pat. No. 5,660,791 (“FluidTesting Sensor for Use in Dispensing Instrument”); U.S. Pat. No.5,759,364 (entitled “Electrochemical Biosensor”); and U.S. Pat. No.5,798,031 (entitled “Electrochemical Biosensor”); each of which isincorporated herein in its entirety.

Turning now to FIG. 5 a, the operation of the lancing and harvestingdevice 26 will be described according to one embodiment of the presentinvention. The lancing and harvesting device 26 is placed against thetest subject's skin S. The containing ring 24 contacts the skin S of thetest subject. In an embodiment of the present invention wherein thelancing and harvesting device 26 is vacuum assisted, the vacuum is usedto draw the skin S of the test subject into contact with the containingring 24.

In FIG. 5 a, the lancet 28 is shown just prior to lancing the skin ofthe test subject. In operation, the lancet 28 passes through (i.e.,punctures) the lid 14 on its way to the skin of the test subject. Whenthe skin S of the test subject is in contact with the containing ring24, the user depresses the plunger 36 which triggers the lancingassembly 31 (FIG. 4). Upon actuation, the lancet 28 pierces the lid 14then proceeds through the collection chamber 16 and pierces the skin Sof test subject. The lance site on the test subject's skin is bounded bythe collection chamber 16 (i.e., within the outer periphery of thecollection chamber 16).

Referring now to FIG. 5 b, the device 26 is shown after piercing the lid14 and while puncturing the test subject's skin S. After the skin S ofthe test subject is pierced, the lancet 28 withdraws from the subject'sskin S as shown in FIG. 5 c. After the withdraw of the lancet 28 fromthe skin S, blood B begins to fill the collection chamber 16. Uponentering the collection chamber 16, some of the blood B begins to enterthe capillary channel 18. As the blood B continues to fill the capillarychannel 18, the blood B contacts the lid 14 as can be seen in FIG. 5 dwhich directs the blood B toward the inlet of the capillary channel 18.The collection chamber 16, bounded by the containing ring 24 and the lid14, collect and contain the blood sample B. Thus, according to oneembodiment of the present invention, the harvesting of the blood sampleis not dependant on any particular blood droplet formation.

Referring now to FIG. 5 e, upon further filling of the collectionchamber 16, the blood B continues to move along the capillary channel 18from the collection chamber 16 towards the test element 20. The blood Bcontacts the test element once it moves into the test area 19. Accordingto the illustrated embodiment of the test strip 10, a vent 22facilitates the movement of the blood B through the capillary channel18, which allows air within the capillary channel 18 to exhaust from thechannel as the blood B fills the channel 18.

As shown in FIG. 5 f, after reaching the end of the capillary channel 18the blood B enters the test area 19 and contacts the test element 20,where the blood B is absorbed. The spacing along side of the testelement 20 increases the exposure of the test element 20 to the blood inthe reaction area, which allows for quicker absorption of the blood B bythe test element 20. Further, if desired, spacing may be provided underor above the test element 20 to further facilitate rapid absorption ofthe blood B as is discussed above. Once the blood B is absorbed by thetest element, the blood mixes with the reagent applied to the testelement 20, which produces a reaction indicative of the concentration ofthe analyte (e.g., glucose) in the blood. If the assay is calorimetricin nature, a light sensor disposed within the end cap 30 measures thecolorimetric reaction. If the assay is electrochemical in nature, ameter measures the amount of current produced by the electrochemicalreaction. After use, in one embodiment, the end cap 30 and the teststrip 10 may be removed from the lancing and harvesting device 26 anddiscarded.

Referring now to FIG. 6, a test strip 50 according to an alternativeembodiment of the present invention is shown. The test strip 50 includesa partially enclosed collection chamber 56 that is formed at one end ofa base 52 of the test strip 50. The partially enclosed collectionchamber 56 may have varying degrees of closure according to alternativeembodiments of the present invention. The test strip 50 includes a lid54 having a lip 57 that extends a distanced from the lid 54. As theblood collects in the partially enclosed collection chamber 56, theblood contacts the lid 54 and lip 57 which directs the blood sampletoward the inlet of the capillary channel 19.

While the test strip has been described thus far as having a two piececonstruction (i.e., a base 12 and a lid 14) with a capillary channel 18formed in the base 12, the test strip 10 can have a three piececonstruction. In such an embodiment, a U-shaped spacer layer is disposedbetween the base 12 and the lid 14 and may be attached to each with anadhesive. The interior of the U-shaped spacer layer forms the side wallsof a capillary channel while the lid and base form the top and bottom,respectively.

While the invention is susceptible to various modifications andalternative forms, specific embodiments thereof have been shown by wayof example in the drawings and are described in detail herein. It shouldbe understood, however, that it is not intended to limit the inventionto the particular forms disclosed, but, to the contrary, the intentionis to cover all modifications, equivalents and alternatives fallingwithin the spirit and scope of the invention as defined by the appendedclaims.

1. A test strip for use in the determination of an analyte in a fluidsample, the test strip comprising: a base having a top and a bottom; acollection chamber extending from the bottom of the base; a containingring disposed on the bottom of the base, the containing ring surroundingthe collection chamber; a capillary channel positioned adjacent to thetop of the base, the capillary channel having an inlet fluidly coupledto the collection chamber; a test area in fluid communication with thecapillary channel; a test element being disposed within the test area;and a lid attached to at least a portion of the top of the base, the lidcovering at least a portion of the collection chamber, the test area,and the capillary channel, wherein the capillary channel extends beyondthe test area to form a vent.
 2. The test strip of claim 1, wherein thelid is constructed of a substantially optically clear material.
 3. Thetest strip of claim 1, wherein the lid is constructed of a substantiallynonporous material.
 4. The test strip of claim 1, wherein the testelement includes a reagent for producing a reaction indicative of theconcentration of the analyte in the fluid sample.
 5. The test strip ofclaim 4, wherein the analyte is glucose.
 6. The test strip of claim 4,wherein the sample is blood.
 7. The test strip of claim 1, incombination with a lancing device.
 8. The test strip of claim 1,comprising a hydrophilic coating disposed on at least a portion of thecapillary channel.
 9. The test strip of claim 1, wherein the testelement is attached to the lid.
 10. The test strip of claim 9, whereinthe test element is attached to the lid with a substantially opticallyclear adhesive.
 11. The test strip of claim 1, wherein a transversedimension of the test area is greater than a transverse dimension of thetest element.
 12. The test strip of claim 1, wherein a depth of the testarea is greater than a thickness of the test element.
 13. The test stripof claim 1, wherein the containing ring outwardly extends from thebottom of the base.
 14. A device for use in the determination of ananalyte in a body fluid, the device including a lancing assembly havinga lancet for puncturing the skin of a test subject, the lancet beingadapted to move between a retracted position and an extended positionfor puncturing the skin of a test subject, the device comprising: an endcap removably attached to the lancing device, the end cap having a rimfor contacting the skin of the test subject, the lancet extending beyondthe rim of the end cap when in the extended position; and a test stripdisposed within the end cap, the test strip including a collectionchamber and a capillary channel fluidly coupled to the collectionchamber, the test strip including a test area in fluid communicationwith the capillary channel, a test element being disposed within thetest area, the capillary channel extending beyond the test area to forma vent, the test strip including a lid disposed over at least a portionof the collection chamber and the capillary channel, the lancetpuncturing the lid and extending through the collection chamber whenmoving between the retracted position and the extended position.
 15. Thedevice of claim 14, wherein the test strip includes a containing ringoutwardly extending from the bottom of the test strip for contacting atest subject's skin.
 16. The device of claim 14, wherein the lancingassembly is vacuum assisted.
 17. The device of claim 14, wherein the lidof the test strip is constructed of a substantially optically clearmaterial.
 18. The device of claim 14, wherein the lid of the test stripconstructed of a substantially nonporous material.
 19. The device ofclaim 14, wherein the test element of the test strip includes a reagentfor producing a reaction indicative of the concentration of the analytein the fluid sample.
 20. The device of claim 19, wherein the analyte isglucose.
 21. The device of claim 19, wherein the sample is blood. 22.The device of claim 19, wherein the reagent produces a colorimetricreaction, the device comprising an optical device for reading thereaction.
 23. The device of claim 19, wherein the reagent produces anelectrochemical reaction, the device comprising a meter for measuringthe reaction.
 24. The device of claim 14, comprising a hydrophiliccoating disposed on at least a portion of the capillary channel of thetest strip.
 25. The device of claim 14, wherein the test element isattached to the lid of the test strip.
 26. The device of claim 25,wherein the test element is attached to the lid of the test strip with asubstantially optically clear adhesive.
 27. The device of claim 14,wherein a transverse dimension of the test area is greater than atransverse dimension of the test element.
 28. The device of claim 14,wherein a depth of the test area is greater than a thickness of the testelement.
 29. The device of claim 14, wherein the test element of thetest strip includes a reagent for producing a reaction indicative of theconcentration of the analyte in the fluid sample.
 30. The test strip ofclaim 1, wherein the test area includes a top and a bottom, the testelement including a raised portion extending from one of the top andbottom of the test area, the raised portion including reagent thereon.31. The device of claim 14, wherein the test area includes a top and abottom, the test element including a raised portion extending from oneof the top and bottom of the test area, the raised portion includingreagent thereon.